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Catalog Number:
17413
CAS Number:
562858-09-7
1-(5-Trifluoromethyl-[1,3,4]thiadiazol-2-yl)piperazine
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$141.41 /250MG
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Product Information

1-(5-Trifluoromethyl-[1,3,4]thiadiazol-2-yl)piperazine is a versatile compound recognized for its unique trifluoromethyl group, which enhances its chemical stability and reactivity. This compound is particularly valuable in pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its structure allows for modifications that can lead to the discovery of new therapeutic agents, making it a crucial component in drug design and development processes.

In addition to its pharmaceutical applications, this compound is also utilized in agrochemical formulations, where its properties can contribute to the development of effective pesticides and herbicides. The trifluoromethyl group imparts desirable characteristics such as increased lipophilicity, which can improve the bioavailability of agrochemicals. Researchers and industry professionals will find this compound beneficial for its potential to enhance the efficacy of their products while maintaining a favorable safety profile.

CAS Number
562858-09-7
Molecular Formula
C7H9F3N4S
Molecular Weight
238.24
MDL Number
MFCD05884941
PubChem ID
2146069
Conditions
Store at 0-8°C
General Information
CAS Number
562858-09-7
Molecular Formula
C7H9F3N4S
Molecular Weight
238.24
MDL Number
MFCD05884941
PubChem ID
2146069
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-(5-Trifluoromethyl-[1,3,4]thiadiazol-2-yl)piperazine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, providing effective pest control solutions with minimal environmental impact, making it a preferred choice for sustainable agriculture.
  • Material Science: Its unique properties allow for the development of advanced materials, such as coatings and polymers, that exhibit improved durability and resistance to environmental degradation.
  • Biochemical Research: Researchers utilize this compound in studies related to enzyme inhibition and receptor binding, contributing to the understanding of biological pathways and disease mechanisms.
  • Fluorinated Compounds: The trifluoromethyl group enhances the compound's stability and lipophilicity, making it valuable in the design of new fluorinated compounds for various applications in medicinal chemistry.

Citations